White Paper

Facilitating Good Clinical Data Review In Your Clinical Trial

GettyImages-576919878-analytics-computer-testing-research-data

Decentralized trials and/or new trial designs are causing a rapid increase in the variety of data sources used in trials. To meet a growing list of guidelines for Good Clinical Practice (GCP), including International Council for Harmonization of Technical Requirements for Pharmaceuticals for Human Use (ICH) E6(R2) and the impending ICH E6(R3) this data must be carefully collected and analyzed.

The biopharma industry will continue to modify clinical trials, which will produce changes in the resulting data. With new kinds of data—likely more complex collections of data, and surely more data—biopharma companies will face increasing needs for software that overcomes challenges from data analysis to overall company performance and product quality.

By centralizing analysis and communications, a biopharma company creates a system based on connectivity and automation, aggregated and usable data, flexible analysis, and methods of collaborative data review.

VIEW THE WHITE PAPER!

Get unlimited access to:

Trend and Thought Leadership Articles
Case Studies & White Papers
Extensive Product Database
Members-Only Premium Content
Welcome Back! Please Log In to Continue. X

Enter your credentials below to log in. Not yet a member of ECM Connection? Subscribe today.

Subscribe to ECM Connection X

Please enter your email address and create a password to access the full content, Or log in to your account to continue.

or

Subscribe to ECM Connection

PerkinElmer Informatics, Inc